Literature DB >> 3334413

Kinetics and mechanism of captopril oxidation in aqueous solution under controlled oxygen partial pressure.

T Y Lee1, R E Notari.   

Abstract

The stability of captopril in aqueous solution at 32 degrees C was studied in the pH range 6.6 to 8.0 under controlled oxygen partial pressure (90-760 mm Hg) with and without the addition of cupric ion. The oxidation product, captopril disulfide, was found to be the sole degradation product. A change in reaction rate from first order to zero order occurs as the captopril concentration decreases. The concentration at which this transition takes place is a function of the pH, oxygen partial pressure, and cupric ion concentration. The apparent first-order rate constants show a first-order dependency on both the oxygen partial pressure and the cupric ion concentration. However, the apparent zero-order rate constants show a first-order dependency on oxygen partial pressure and a second-order dependency on cupric ion concentration. As the pH increases from 6.6 to 8.0, the first-order process becomes more predominant. A mechanism which consists of cupric ion- and molecular oxygen-catalyzed oxidation is proposed to explain those observations.

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Year:  1987        PMID: 3334413     DOI: 10.1023/a:1016406716989

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  6 in total

1.  Kinetics of degradation in solution of epinephrine by molecular oxygen.

Authors:  T D SOKOLOSKI; T HIGUCHI
Journal:  J Pharm Sci       Date:  1962-02       Impact factor: 3.534

2.  Kinetics of copper catalyzed oxidation of 2, 3-dimercapto-1-propanol by molecular oxygen.

Authors:  E G RIPPIE; T HIGUCHI
Journal:  J Pharm Sci       Date:  1962-07       Impact factor: 3.534

3.  Kinetics of reaction between molecular oxygen and 2, 3-dimercapto-1-propanol in aqueous solution.

Authors:  E G RIPPIE; T HIGUCHI
Journal:  J Pharm Sci       Date:  1962-08       Impact factor: 3.534

4.  Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acids.

Authors:  D W Cushman; H S Cheung; E F Sabo; M A Ondetti
Journal:  Biochemistry       Date:  1977-12-13       Impact factor: 3.162

5.  Determination of captopril in blood and urine by high-performance liquid chromatography.

Authors:  Y Kawahara; M Hisaoka; Y Yamazaki; A Inage; T Morioka
Journal:  Chem Pharm Bull (Tokyo)       Date:  1981-01       Impact factor: 1.645

6.  A specific orally active inhibitor of angiotensin-converting enzyme in man.

Authors:  R K Ferguson; G A Turini; H R Brunner; H Gavras; D N McKinstry
Journal:  Lancet       Date:  1977-04-09       Impact factor: 79.321

  6 in total
  1 in total

1.  Reaction of N-Acetylcysteine with Cu2+: Appearance of Intermediates with High Free Radical Scavenging Activity: Implications for Anti-/Pro-Oxidant Properties of Thiols.

Authors:  Ivan Valent; Lucie Bednárová; Igor Schreiber; Juraj Bujdák; Katarína Valachová; Ladislav Šoltés
Journal:  Int J Mol Sci       Date:  2022-05-31       Impact factor: 6.208

  1 in total

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